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Development and validation of a whole-exome sequencing test for simultaneous detection of point mutations, indels and copy-number alterations for precision cancer care.
Rennert H, Eng K, Zhang T, Tan A, Xiang J, Romanel A, Kim R, Tam W, Liu YC, Bhinder B, Cyrta J, Beltran H, Robinson B, Mosquera JM, Fernandes H, Demichelis F, Sboner A, Kluk M, Rubin MA, Elemento O. Rennert H, et al. Among authors: kluk m. NPJ Genom Med. 2016;1:16019-. doi: 10.1038/npjgenmed.2016.19. Epub 2016 Jul 20. NPJ Genom Med. 2016. PMID: 28781886 Free PMC article.
Comparison of Multiple Clinical Testing Modalities for Assessment of NPM1-Mutant AML.
Lopez A, Patel S, Geyer JT, Racchumi J, Chadburn A, Simonson P, Ouseph MM, Inghirami G, Mencia-Trinchant N, Guzman ML, Gomez-Arteaga A, Lee S, Desai P, Ritchie EK, Roboz GJ, Tam W, Kluk MJ. Lopez A, et al. Among authors: kluk mj. Front Oncol. 2021 Aug 30;11:701318. doi: 10.3389/fonc.2021.701318. eCollection 2021. Front Oncol. 2021. PMID: 34527579 Free PMC article.
Successful treatment and integrated genomic analysis of an infant with FIP1L1-RARA fusion-associated myeloid neoplasm.
Miltiadous O, Petrova-Drus K, Kaicker S, Mathew S, Kluk M, Geyer JT, Rodriguez-Sanchez I, Bouvier N, Inghirami G, Stieglitz E, Khedoudja N, Benayed R, Richardson M, Anderson W, Benhamida J, You D, Londono D, Kung AL, Prockop SE, Roshal M, Zhang Y, Shukla N. Miltiadous O, et al. Among authors: kluk m. Blood Adv. 2022 Feb 22;6(4):1137-1142. doi: 10.1182/bloodadvances.2021004966. Blood Adv. 2022. PMID: 34551074 Free PMC article.
NPM1 Biology in Myeloid Neoplasia.
Patel SS, Kluk MJ, Weinberg OK. Patel SS, et al. Curr Hematol Malig Rep. 2020 Aug;15(4):350-359. doi: 10.1007/s11899-020-00592-3. Curr Hematol Malig Rep. 2020. PMID: 32494951 Review.
77 results